Pneumonia, chronic obstructive pulmonary disease, interstitial pneumonia, respiratory failure, pulmo
Conditions
Interventions
A total of two questionnaire surveys will be conducted, one before the use of the nasal cannula fixing device, and one week or more and less than two weeks after the use of the nasal cannula fixing de
Sponsors
Tsuruta Kaori
Medical Project Co,.Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Patients who are hospitalized at Showa University Hospital, Showa University Hospital East, or Showa University Koto Toyosu Hospital and have been using a nasal cannula for more than one week. 2) Patients who can be surveyed by questionnaire 3)Patients who have given written informed consent to participate in this study 4)Patients aged 18 years or older at the time of informed consent
Exclusion criteria
Exclusion criteria: 1) Patients with severe mental illness 2) Patients for whom questionnaire survey is impossible 3) Patients judged to be ineligible by the judgment of the research director and co-investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Presence or absence of medical device-related pressure injuries due to nasal cannula fixation devices | — |
Secondary
| Measure | Time frame |
|---|---|
| Differences between nasal cannulas alone and when using fixtures: Discomfort, auricular pain, fit of nasal cannula, presence/absence/change in ease of removal of nasal cannula Usability of the nasal cannula fixing device: ease of wearing the fixing device, whether you want to continue using it in the future In addition, each evaluation item is based on patient background sex, age, disease name, BMI, presence or absence of home oxygen, hospitalization date, start date of nasal cannula use, etc. | — |
Contacts
Public ContactKaori Tsuruta
Department of Physical Therapy
Outcome results
None listed